About: Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent

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About: Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent Goto Sponge NotDistinct Permalink

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scientific article published on 01 January 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique (publié 2007) (fr) наукова стаття, опублікована у квітні 2007 (uk) im Jahr 2007 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xineru de 2007 (ast) artikull shkencor i botuar më 01 janar 2007 (sq) scientific article published on 01 January 2007 (en)
publication date	wds:Q64168894-2C6F4842-697F-4020-B408-036FF542C8DF
publication date	2007-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q64168894-C86BDB24-5AD4-4815-B080-DB3C20BEF81D
language of work or name	English
author name string	wds:Q64168894-962240E5-29CD-48F8-A77F-96840FFF4FED wds:Q64168894-AD548ACB-26FD-4C92-B8E9-19869B7921D8 wds:Q64168894-B3406197-0031-45ED-B367-0B0E3B6D1656
author name string	Patricia Moriel Martin A Ariger Christian Defieber
rdfs:label	Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent (en) Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent (nl) Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent (sq)
skos:prefLabel	Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent (en) Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent (nl) Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent (sq)
name	Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent (en) Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent (nl) Iridium-Catalyzed Synthesis of Primary Allylic Amines from Allylic Alcohols: Sulfamic Acid as Ammonia Equivalent (sq)
author	wds:Q64168894-45300F8E-EED9-444A-870A-95EEB3023988
author	Erick Moran Carreira
title	wds:Q64168894-10DF90B2-F720-4ACC-8C71-07382FA735EA
title	Iridium-catalyzed synthesis of primary allylic amines from allylic alcohols: sulfamic acid as ammonia equivalent (en)
page(s)	wds:Q64168894-F46D78F9-2DE9-46CC-96B0-E8CAE20F56B0
page(s)	3139-3143
instance of	wds:Q64168894-7DC49939-5C12-487C-B52F-31E68CFEE2C6
instance of	scholarly article
main subject	wds:Q64168894-4560AD9C-8B20-40B5-98A1-79933B51700C wds:Q64168894-7E9A4CA8-2F96-41DA-B130-0D9E29B9170A
main subject	iridium wd:Q4087
PubMed ID	wds:Q64168894-55000F32-5E47-4B73-967B-ED64BB5795BB
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17352000
PubMed ID	17352000
published in	wds:Q64168894-FEA018E5-B55A-4EF0-A3E3-471722408104
published in	Angewandte Chemie International Edition
issue	wds:Q64168894-CB6989E1-C52F-4255-8F77-C84D0055881D
volume	wds:Q64168894-D5C3A08F-6BCA-4FED-BFD5-15949DE0A494
issue	17
volume	46
DOI	wds:Q64168894-401CCCD1-B975-457B-B836-02E376F9755C
DOI	http://dx.doi.org/10.1002/ANIE.200700159
DOI	10.1002/ANIE.200700159
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q64168894
is cites work of	Gold(I)-catalyzed enantioselective intramolecular dehydrative amination of allylic alcohols with carbamates Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols Phosphoramidites: privileged ligands in asymmetric catalysis Gold(I)-catalyzed intramolecular amination of allylic alcohols with alkylamines Gold(I)-catalyzed amination of allylic alcohols with cyclic ureas and related nucleophiles Chiral NHC-catalyzed oxodiene Diels-Alder reactions with alpha-chloroaldehyde bisulfite salts Intermolecular hydroamination of allenes with N-unsubstituted carbamates catalyzed by a gold(I) N-heterocyclic carbene complex Regio- and enantioselective N-allylations of imidazole, benzimidazole, and purine heterocycles catalyzed by single-component metallacyclic iridium complexes Enantioselective, iridium-catalyzed monoallylation of ammonia Iridium-catalyzed asymmetric intramolecular allylic amidation: enantioselective synthesis of chiral tetrahydroisoquinolines and saturated nitrogen heterocycles Enantioselective Synthesis of Acyclic α-Quaternary Carboxylic Acid Derivatives through Iridium-Catalyzed Allylic Alkylation. Palladium-Catalyzed Anti-Markovnikov Oxidation of Allylic Amides to Protected β-Amino Aldehydes. Direct, intermolecular, enantioselective, iridium-catalyzed allylation of carbamates to form carbamate-protected, branched allylic amines Amphiphilic π-Allyliridium C,O-Benzoates Enable Regio- and Enantioselective Amination of Branched Allylic Acetates Bearing Linear Alkyl Groups. Uncovering the psychoactivity of a cannabinoid from liverworts associated with a legal high Titanium-mediated reductive cross-coupling reactions of imines with terminal alkynes: An efficient route for the synthesis of stereodefined allylic amines Rhodium-catalyzed asymmetric hydroamination and hydroindolation of keto-vinylidenecyclopropanes. Synergistic catalysis for cascade allylation and 2-aza-cope rearrangement of azomethine ylides Regio- and Enantioselective Iridium-Catalyzed Amination of Racemic Branched Alkyl-Substituted Allylic Acetates with Primary and Secondary Aromatic and Heteroaromatic Amines Delayed catalyst function enables direct enantioselective conversion of nitriles to NH2-amines Iridium-Catalyzed Enantioselective Intermolecular Indole C2-Allylation
is cites work of	wds:Q38586550-15E983CE-B337-41F3-917F-09ABE4B9F97A wds:Q47908622-AA43A316-94B3-43BB-A71F-FCB27E9F4470 wds:Q42249778-4B219B0E-507B-4D55-98BA-B54AEECC7335 wds:Q83174790-39EA2ACB-D5E6-40AF-9D09-33646A3FE330 wds:Q33545287-8C359E74-3711-49EC-B128-3AFA4D0321DE wds:Q39706710-2B1162E3-ADFF-4090-B89C-F5FD123E302A wds:Q47709708-8B9C76E5-F36A-4450-B180-B3EE74457E9C wds:Q58569579-85826071-76AE-4BD7-A64A-EE58D232729E wds:Q36773808-60CB0F0E-577A-48AC-B8DB-95D5D865D97C wds:Q55334217-A00B72AA-BE99-4C32-BAF6-7ACD924EB348 wds:Q37309821-CB210D45-D728-4FAF-9815-D25587E4C38B wds:Q42466927-18B105E5-788D-4989-AD72-FDA538C9699D wds:Q42321608-059A32CA-B307-4B8B-9049-34929B1A48F3 wds:Q90666165-F263A8F6-78C1-4217-A09B-F4D2ABA4AAA6 wds:Q92859750-695972C4-8C1F-41EA-B2B8-287FB5E85283 wds:Q64067655-67657FB4-C078-4F94-BDB8-30E401AA62B9 wds:Q89853867-D18FFB3E-C078-432E-BEC3-AB12BBACB89D wds:Q42321610-596739C6-8B04-40AD-A158-EE76EA2DB602 wds:Q41771980-7FAC1CBA-9A67-4682-B8E5-42C02BA5D8CD wds:Q51014161-D6BA689D-3DD7-44F5-BAC4-4454E6191C4D wds:Q42170323-2335086A-75C8-4973-A8CF-A4C14452C9A8

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